Valeant Pharmaceuticals

Quality Assurance Associate

US-GA-Union City
Job ID
7606
Pos. Category
R&D
Pos. Type
Full Time

Overview

Performs a wide variety of QA activities to ensure compliance with applicable regulatory requirements

Responsibilities

Assists with GMP internal and external audits.

Assists with training programs.

Performs batch records review.

Perform disposition of product.

Coordinates data and documentation review and analysis.

Processes deviations and non-conformances.

Writes documents, standard operating procedures and reports.

Represents department in cross-functional teams, projects and GXP-related problem resolution.

 

Working Conditions:

 

Ability to sit or stand for extended periods of time 

Intermittent walking to gain access to work areas

Finger dexterity sufficient to use a computer and to complete paperwork activities

Vision sufficient to use a computer, to read written materials and to complete paperwork activities;

Hearing sufficient to communicate with individuals by telephone and in person

Ability to lift up to 25 pounds.

 

May be required to work alternate shifts

Ability to gown aseptically for work in Clean Room environments

Job performed in a lab, office, or utility (noisy) environment

Must have the ability to work around laboratories, manufacturing areas and equipment with exposure to blood, blood products or OPIM (other potentially infectious materials) while donning required personal protective materials.

Regularly lift 10-20 lbs. and occasionally lift up to 50 lbs.

 

 

Scope of position:

 

  • Uses professional concepts and company policies and procedures to solve a variety of problems.
  • Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. Exercises judgment within defined procedures and practices to determine appropriate action.
  • Normally receives general instructions on routine work, detailed instructions on new assignments.

 

key relationships:

  • Manufacturing Department
  • Quality Control Department
  • Regulatory officials

Qualifications

  • Bachelor’s degree in a scientific discipline or equivalent.
  • Proficient in MS Office applications.
  • GMP or regulated environment experience is preferable

Be Aware of Recruiting Fraud

Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.

 

To learn more please read Valeant’s Job Offer Fraud Statement.

 

 

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